Exchange Flashcards

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1
Q

How does an organism’s size relate to their surface area to volume ratio?

A

The larger the organism, the lower the surface area to volume ratio.

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2
Q

How does an organism’s surface area to volume ratio relate to their metabolic rate?

A

The smaller the surface area to volume ratio, the higher the metabolic rate.

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3
Q

How might a large organism adapt to compensate for its small surface area to volume ratio?

A

Changes that increase surface area e.g. folding; body parts become larger e.g. elephant’s ears; elongating shape; developing a specialised gas exchange surface.

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4
Q

Why do multicellular organisms require specialised gas exchange surfaces?

A

Their smaller surface area to volume ratio means the distance that needs to be crossed is larger and substances cannot easily enter the cells as in a single-celled organism.

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5
Q

Name three features of an efficient gas exchange surface.

A
  1. Large surface area, e.g. folded membranes in mitochondria.
  2. Thin/short distance, e.g. wall of capillaries.
  3. Steep concentration gradient, maintained by blood supply or ventilation, e.g. alveoli.
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6
Q

Why can’t insects use their bodies as an exchange surface?

A

They have a waterproof chitin exoskeleton and a small surface area to volume ratio in order to conserve water.

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7
Q

Name and describe the three main features of an insect’s gas transport system.

A

● Spiracles= holes on the body’s surface which may be opened or closed by a valve for gas or water exchange.

● Tracheae= large tubes extending through all body tissues, supported by rings to prevent collapse.

● Tracheoles= smaller branches dividing off the tracheae.

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8
Q

Explain the process of gas exchange in insects.

A

● Gases move in and out of the tracheae through the spiracles.

● A diffusion gradient allows oxygen to diffuse into
the body tissue while waste CO2 diffuses out.

● Contraction of muscles in the tracheae allows
mass movement of air in and out.

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9
Q

Why can’t fish use their bodies as an exchange surface?

A

They have a waterproof, impermeable outer membrane and a small surface area to volume ratio.

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10
Q

Name and describe the two main features of a fish’s gas transport system.

A

Gills= located within the body, supported by arches, along which are multiple projections of gill filaments, which are stacked up in piles.

Lamellae= at right angles to the gill filaments, give an increased surface area. Blood and water flow across them in opposite directions (countercurrent exchange system).

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11
Q

Explain the process of gas exchange in fish.

A

● The fish opens its mouth to enable water to flow in, then closes its mouth to increase pressure.

● The water passes over the lamellae, and the oxygen diffuses into the bloodstream.

● Waste carbon dioxide diffuses into the water and flows back out of the gills.

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12
Q

How does the countercurrent exchange system maximise oxygen absorbed by the fish?

A

Maintains a steep concentration gradient, as water is always next to blood of a lower oxygen concentration. Keeps rate of diffusion constant and enables 80% of available oxygen to be absorbed.

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13
Q

Name and describe three adaptations of a leaf that allow efficient gas exchange.

A
  1. Thin and flat to provide short diffusion pathway and large surface area to volume ratio.
  2. Many minute pores in the underside of the leaf (stomata) allow gases to easily enter.
  3. Air spaces in the mesophyll allow gases to move around the leaf, facilitating photosynthesis.
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14
Q

How do plants limit their water loss while still allowing gases to be exchanged?

A

Stomata regulated by guard cells which allows them to open and close as needed. Most stay closed to prevent water loss while some open to let oxygen in.

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15
Q

Describe the pathway taken by air as it enters the mammalian gaseous exchange system.

A

Nasal cavity → trachea → bronchi → bronchioles → alveoli

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16
Q

Describe the function of the nasal cavity in the mammalian gaseous exchange system.

A

A good blood supply warms and moistens the air entering the lungs. Goblet cells in the membrane secrete mucus which traps dust and bacteria.

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17
Q

Describe the trachea and its function in the mammalian gaseous exchange system.

A

● Wide tube supported by C-shaped cartilage to keep the air passage open during pressure changes.

● Lined by ciliated epithelium cells which move mucus towards the throat to be swallowed, preventing lung infections.

● Carries air to the bronchi.

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18
Q

Describe the bronchi and their function in the mammalian gaseous exchange system.

A

● Like the trachea they are supported by rings of cartilage and are lined by ciliated epithelium cells.

● However, they are narrower and there are two of them, one for each lung.

● Allow passage of air into the bronchioles.

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19
Q

Describe the bronchioles and their function in the mammalian gaseous exchange system.

A

● Narrower than the bronchi.

● Do not need to be kept open by cartilage, therefore mostly have only muscle and elastic fibres so that they can contract and relax easily during ventilation.

● Allow passage of air into the alveoli.

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20
Q

Describe the alveoli and their function in the mammalian gaseous exchange system.

A

● Mini air sacs, lined with epithelium cells, site of gas exchange.

● Walls only one cell thick, covered with a network of capillaries, 300 million in each lung, all of which facilitates gas diffusion.

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21
Q

Explain the process of inspiration and the changes that occur throughout the thorax.

A

● External intercostal muscles contract (while internal relax), pulling the ribs up and out.

● Diaphragm contracts and flattens.

● Volume of the thorax increases.

● Air pressure outside the lungs is therefore higher than the air pressure inside, so air moves in to rebalance.

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22
Q

Explain the process of expiration and the changes that occur throughout the thorax.

A

● External intercostal muscles relax (while internal contract), bringing the ribs down and in.

● Diaphragm relaxes and domes upwards.

● Volume of the thorax decreases.

● Air pressure inside the lungs is therefore higher than the air pressure outside, so air moves out to rebalance.

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23
Q

What is tidal volume?

A

The volume of air we breathe in and out during each breath at rest.

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24
Q

What is breathing rate?

A

The number of breaths we take per minute.

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25
Q

How do you calculate pulmonary ventilation rate?

A

Tidal volume x breathing rate. These can be measured using a spirometer, a device which records volume changes onto a graph as a person breathes.

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26
Q

Define digestion.

A

The hydrolysis of large, insoluble molecules into smaller molecules that can be absorbed across cell membranes.

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27
Q

Which enzymes are involved in carbohydrate digestion? Where are they found?

A

● Amylase in mouth

● Maltase, sucrase, lactase in membrane of small intestine

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28
Q

What are the substrates and products of the carbohydrate digestive enzymes?

A

● Amylase → starch into smaller polysaccharides

● Maltase → maltose into 2 x glucose

● Sucrase → sucrose into glucose and fructose

● Lactase → lactose into glucose and galactose

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29
Q

Where are lipids digested?

A

The small intestine.

30
Q

What needs to happen before lipids can be digested?

A

They must be emulsified by bile salts produced by the liver. This breaks down large fat molecules into smaller, soluble molecules called micelles, increasing surface area.

31
Q

How are lipids digested?

A

Lipase hydrolyses the ester bond between the monoglycerides and fatty acids.

32
Q

Which enzymes are involved in protein digestion? What is their role?

A

● Endopeptidases= break between specific amino acids in the middle of a polypeptide.

● Exopeptidases= break between specific amino acids at the end of a polypeptide.

● Dipeptidases= break dipeptides into amino acids.

33
Q

How are certain molecules absorbed into the ileum despite a negative concentration gradient?

A

Through co-transport.

34
Q

Which molecules require co-transport?

A

Amino acids and monosaccharides.

35
Q

Explain how sodium ions are involved in co-transport.

A

Sodium ions (Na+) are actively transported out of the cell into the lumen, creating a diffusion gradient. Nutrients are then taken up into the cells along with Na+ ions.

36
Q

Why do fatty acids and monoglycerides not require co-transport?

A

The molecules are nonpolar, meaning they can easily diffuse across the membrane of the epithelial cells.

37
Q

Describe the structure of haemoglobin.

A

Globular, water soluble. Consists of four polypeptide chains, each carrying a haem group (quaternary structure).

38
Q

Describe the role of haemoglobin.

A

Present in red blood cells. Oxygen molecules bind to the haem groups and are carried around the body to where they are needed in respiring tissues.

39
Q

Name three factors affecting oxygen-haemoglobin binding.

A
  1. Partial pressure/concentration of oxygen.
  2. Partial pressure/concentration of carbon dioxide.
  3. Saturation of haemoglobin with oxygen.
40
Q

How does partial pressure of oxygen affect oxygen-haemoglobin binding?

A

As partial pressure of oxygen increases, the affinity of haemoglobin for oxygen also increases, so oxygen binds tightly to haemoglobin. When partial pressure is low, oxygen is released from haemoglobin.

41
Q

How does partial pressure of carbon dioxide affect oxygen-haemoglobin binding?

A

As partial pressure of carbon dioxide increases, the conditions become acidic causing haemoglobin to change shape. The affinity of haemoglobin for oxygen therefore decreases, so oxygen is released from haemoglobin. This is known as the Bohr effect.

42
Q

How does saturation of haemoglobin with oxygen affect oxygen-haemoglobin binding?

A

It is hard for the first oxygen molecule to bind. Once it does, it changes the shape to make it easier for the second and third molecules to bind, known as positive cooperativity. It is then slightly harder for the fourth oxygen molecule to bind because there is a low chance of finding a binding site.

43
Q

Explain why oxygen binds to haemoglobin in the lungs.

A

● Partial pressure of oxygen is high.

● Low concentration of carbon dioxide in the lungs, so affinity is high.

● Positive cooperativity (after the first oxygen molecule binds, binding of subsequent molecules is easier).

44
Q

Explain why oxygen is released from haemoglobin in respiring tissues.

A

● Partial pressure of oxygen is low

● High concentration of carbon dioxide in respiring tissues, so affinity decreases.

45
Q

What do oxyhaemoglobin dissociation curves show?

A

Saturation of haemoglobin with oxygen (in %), plotted against partial pressure of oxygen (in kPa). Curves further to the left show the haemoglobin has a higher affinity for oxygen.

46
Q

How does carbon dioxide affect the position of an oxyhaemoglobin dissociation curve?

A

Curve shifts to the right because haemoglobin’s affinity for oxygen has decreased.

47
Q

Name three common features of a mammalian circulatory system.

A
  1. Suitable medium for transport, water-based to allow substances to dissolve.
  2. Means of moving the medium and maintaining pressure throughout the body, such as the heart.
  3. Means of controlling flow so it remains unidirectional, such as valves.
48
Q

Relate the structure of the chambers to their function.

A

● Atria: thin-walled and elastic, so they can stretch when filled with blood

● Ventricles: thick muscular walls pump blood under high pressure. The left ventricle is thicker than the right because it has to pump blood all the way around the body.

49
Q

Relate the structure of the vessels to their function.

A

● Arteries have thick walls to handle high pressure without tearing, and are muscular and elastic to control blood flow.

● Veins have thin walls due to lower pressure, therefore requiring valves to ensure blood doesn’t flow backwards. Have less muscular and elastic tissue as they don’t have to control blood flow.

50
Q

Why are two pumps (left and right) needed instead of one?

A

To maintain blood pressure around the whole body. When blood passes through the narrow capillaries of the lungs, the pressure drops sharply and therefore would not be flowing strongly enough to continue around the whole body. Therefore it is returned to the heart to increase the pressure.

51
Q

Describe what happens during cardiac diastole.

A

The heart is relaxed. Blood enters the atria, increasing the pressure and pushing open the atrioventricular valves. This allows blood to flow into the ventricles. Pressure in the heart is lower than in the arteries, so semilunar valves remain closed.

52
Q

Describe what happens during atrial systole.

A

The atria contract, pushing any remaining blood into the ventricles.

53
Q

Describe what happens during ventricular systole.

A

The ventricles contract. The pressure increases, closing the atrioventricular valves to prevent backflow, and opening the semilunar valves. Blood flows into the arteries.

54
Q

Name the nodes involved in heart contraction and where they are situated.

A

● Sinoatrial node (SAN)= wall of right atrium.

● Atrioventricular node (AVN)= in
between the two atria.

55
Q

What does myogenic mean?

A

The heart’s contraction is initiated from within the muscle itself, rather than by nerve impulses.

56
Q

Explain how the heart contracts.

A

● SAN initiates and spreads impulse across the atria, so they contract.

● AVN receives, delays, and then conveys the impulse down the bundle of His.

● Impulse travels into the Purkinje fibres which branch across the ventricles, so they contract from the bottom up.

57
Q

Why does the impulse need to be delayed?

A

If the impulse spread straight from the atria into the ventricles, there would not be enough time for all the blood to pass through and for the valves to close.

58
Q

How is the structure of capillaries suited to their function?

A

● Walls are only one cell thick; short diffusion pathway.

● Very narrow, so can permeate tissues and red blood cells can lie flat against the wall, effectively delivering oxygen to tissues.

● Numerous and highly branched, providing a large surface area.

59
Q

What is tissue fluid?

A

A watery substance containing glucose, amino acids, oxygen, and other nutrients. It supplies these to the cells, while also removing any waste materials.

60
Q

How is tissue fluid formed?

A

As blood is pumped through increasingly small vessels, this creates hydrostatic pressure which forces fluid out of the capillaries. It bathes the cells, and then returns to the capillaries when the hydrostatic pressure is low enough.

61
Q

How is water transported in plants?

A

Through xylem vessels; long, continuous columns that also provide structural support to the stem.

62
Q

Explain the cohesion-tension theory.

A

Water molecules form hydrogen bonds with each other, causing them to ‘stick’ together (cohesion). The surface tension of the water also creates this sticking effect. Therefore as water is lost through transpiration, more can be drawn up the stem.

63
Q

What are the three components of phloem vessels?

A

● Sieve tube elements= form a tube to transport sucrose in the dissolved form of sap.

● Companion cells= involved in ATP production for active loading of sucrose into sieve tubes.

● Plasmodesmata= gaps between cell walls where the cytoplasm links, allowing substances to flow.

64
Q

Name the process whereby organic materials are transported around the plant.

A

Translocation

65
Q

How does sucrose in the leaf move into the phloem?

A

Sucrose enters companion cells of the phloem vessels by active loading, which uses ATP and a diffusion gradient of hydrogen ions. Sucrose then diffuses from companion cells into the sieve tube elements through the plasmodesmata.

66
Q

How do phloem vessels transport sucrose around the plant?

A

As sucrose moves into the tube elements, water potential inside the phloem is reduced. This causes water to enter via osmosis from the xylem and increases hydrostatic pressure. Water moves along the sieve tube towards areas of lower hydrostatic pressure. Sucrose diffuses into surrounding cells where it is needed.

67
Q

Give evidence for the mass flow hypothesis of translocation.

A

● Sap is released when a stem is cut, therefore there must be pressure in the phloem.

● There is a higher sucrose concentration in the leaves than the roots.

● Increasing sucrose levels in the leaves results in increased sucroses in the phloem.

68
Q

Give evidence against the mass flow hypothesis of translocation.

A

● The structure of sieve tubes seems to hinder mass flow.

● Not all solutes move at the same speed, as they would in mass flow.

● Sucrose is delivered at the same rate throughout the plant, rather than to areas with the lowest sucrose concentration first.

69
Q

How can ringing experiments be used to investigate transport in plants?

A

The bark and phloem of a tree are removed in a ring, leaving behind the xylem. Eventually the tissues above the missing ring swells due to accumulation of sucrose as the tissue below begins to die. Therefore sucrose must be transported in the phloem.

70
Q

How can tracing experiments be used to investigate transport in plants?

A

Plants are grown in the presence of radioactive CO2, which will be incorporated into the plant’s sugars. Using autoradiography, we can see that the areas exposed to radiation correspond to where the phloem is.